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Select item 49706011.

rs4970601 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:38554282 (GRCh38)
1:39019954 (GRCh37)
Canonical SPDI:: NC_000001.11:38554281:C:T
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0./0 (HapMap)
T=0.000007/1 (GnomAD_genomes)
T=0.000026/7 (TOPMED)
HGVS:: NC_000001.11:g.38554282C>T, NC_000001.10:g.39019954C>T

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